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Author Sukegawa, Shintaro| Kanno, Takahiro| Yamamoto, Norio| Nakano, Keisuke| Takabatake, Kiyofumi| Kawai, Hotaka| Nagatsuka, Hitoshi| Furuki, Yoshihiko|
Keywords mandibular condylar fracture unsintered hydroxyapatite poly-l-lactide composite plate bioactive resorbable plate biomechanical loading evaluation fracture fixation
Published Date 2019-05-13
Publication Title Materials
Volume volume12
Issue issue9
Publisher MDPI
Start Page 1557
ISSN 1996-1944
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 by the authors.
File Version publisher
PubMed ID 31085981
DOI 10.3390/ma12091557
Web of Science KeyUT 000469757500198
Related Url isVersionOf https://doi.org/10.3390/ma12091557
FullText URL fulltext.pdf
Author Nakano, Masahito| Mukaihara, Takafumi|
Keywords Ralstonia solanacearum type III effector jasmonic acid salicylic acid Nicotiana plants
Published Date 2019-11-28
Publication Title International Journal of Molecular Sciences
Volume volume20
Issue issue23
Publisher MDPI
Start Page 5992
ISSN 1422-0067
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 by the authors.
File Version publisher
PubMed ID 31795135
DOI 10.3390/ijms20235992
Web of Science KeyUT 000504428300174
Related Url isVersionOf https://doi.org/10.3390/ijms20235992
FullText URL NCN7_5_288.pdf Fig.pdf
Author Nakano, Yumiko| Tsunoda, Keiichiro| Yamashita, Toru| Mitsui, Jun| Sato, Kota| Takemoto, Mami| Hishikawa, Nozomi| Ohta, Yasuyuki| Toda, Tatsushi| Tsuji, Shoji| Abe, Koji|
Keywords anti-cholinesterase drug the CHRNE gene congenital myasthenic syndrome late presentation mimicking seronegative myasthenia gravis
Note "This is the peer reviewed version of the following article: Yumiko Nakano et. al. Late presented congenital myasthenic syndrome with novel compound heterozygous CHRNE mutations mimicking seronegative myasthenia gravis. Neurology and Clinical Neuroscience (2019) 7(5) 288-290, which has been published in final form at https://doi.org/10.1111/ncn3.12317. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions."|
Published Date 2019-06-29
Publication Title Neurology and Clinical Neuroscience
Volume volume7
Issue issue5
Publisher Wiley
Start Page 288
End Page 290
ISSN 2049-4173
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
DOI 10.1111/ncn3.12317
Web of Science KeyUT 000476042100001
Related Url isVersionOf https://doi.org/10.1111/ncn3.12317
FullText URL JNR97_5_607.pdf Fig.pdf Fig_sup.pdf Table.pdf
Author Ohta, Yasuyuki| Nomura, Emi| Shang, Jingwei| Feng, Tian| Huang, Yong| Liu, Xia| Shi, Xiaowen| Nakano, Yumiko| Hishikawa, Nozomi| Sato, Kota| Takemoto, Mami| Yamashita, Toru| Abe, Koji|
Keywords ALS SOD1 edaravone in vivo imaging nrf2 oxidative stress
Published Date 2018-12-19
Publication Title Journal of Neuroscience Research
Volume volume97
Issue issue5
Publisher Wiley
Start Page 607
End Page 609
ISSN 0360-4012
NCID AA00703378
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 30565312
DOI 10.1002/jnr.24368
Web of Science KeyUT 000461891200008
Related Url isVersionOf https://doi.org/10.1002/jnr.24368
FullText URL SR9_1_10956.pdf
Author Yamashita, Toru| Shang, Jingwei| Nakano, Yumiko| Morihara, Ryuta| Sato, Kota| Takemoto, Mami| Hishikawa, Nozomi| Ohta, Yasuyuki| Abe, Koji|
Published Date 2019-07-29
Publication Title Scientific Reports
Volume volume9
Issue issue1
Publisher NPG
Start Page 10956
ISSN 2045-2322
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Author(s) 2019
File Version publisher
PubMed ID 31358888
DOI 10.1038/s41598-019-47482-0
Web of Science KeyUT 000477701800059
Related Url isVersionOf https://doi.org/10.1038/s41598-019-47482-0
FullText URL JAD68_4_1667.pdf Fig.pdf
Author Shi, Xiaowen | Liu, Xia| Shang, Jingwei| Morihara, Ryuta| Nakano, Yumiko| Feng, Tian| Huang, Yong| Sato, Kota| Takemoto, Mami| Hishikawa, Nozomi| Yamashita, Toru| Abe, Koji|
Keywords AHSG APP23 mice ITIH4 alzheimer’s disease hypoperfusion inflammation
Published Date 2019-04-23
Publication Title Journal of Alzheimer's Disease
Volume volume68
Issue issue4
Publisher IOS Press
Start Page 1667
End Page 1675
ISSN 1387-2877
NCID AA11545428
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 30958362
DOI 10.3233/JAD-181218
Web of Science KeyUT 000465612500029
Related Url isVersionOf https://doi.org/10.3233/JAD-181218
FullText URL JAD71_1_327.pdf
Author Feng, Tian| Yamashita, Toru| Shang, Jingwei| Shi, Xiaowen| Nakano, Yumiko| Morihara, Ryuta| Tsunoda, Keiichiro| Nomura, Emi| Sasaki, Ryo| Tadokoro, Koh| Matsumoto, Namiko| Hishikawa, Nozomi| Ohta, Yasuyuki| Abe, Koji|
Keywords Alzheimer’s disease chronic cerebral hypoperfusion edaravone neural oxidative stress neuroinflammation neuronal loss
Note The final publication is available at IOS Press through https://doi.org/10.3233/JAD-190369|
Published Date 2019-09-03
Publication Title Journal of Alzheimer's Disease
Volume volume71
Issue issue1
Publisher IOS Press
Start Page 327
End Page 339
ISSN 1387-2877
NCID AA11545428
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 31403949
DOI 10.3233/JAD-190369
Web of Science KeyUT 000484216500026
Related Url isVersionOf https://doi.org/10.3233/JAD-190369
FullText URL JBMRA_107_5_1021.pdf
Author Kunitomi, Yosuke| Hara, Emilio Satoshi| Okada, Masahiro| Nagaoka, Noriyuki| Kuboki, Takuo| Nakano, Takayoshi| Kamioka, Hiroshi| Matsumoto, Takuya|
Keywords apatite bioinspired mineralization bone hydrogel matrix vesicle nanofragments
Published Date 2019-01-24
Publication Title Journal of Biomedical Materials Research Part A
Volume volume107
Issue issue5
Publisher Wiley
Start Page 1021
End Page 1030
ISSN 1549-3296
NCID AA11881516
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 The Authors.
File Version publisher
PubMed ID 30675987
DOI 10.1002/jbm.a.36618
Web of Science KeyUT 000462623800012
Related Url isVersionOf https://doi.org/10.1002/jbm.a.36618
FullText URL J_MedChem_62_19_8809.pdf si_001.pdf si_002.csv
Author Yamada, Shoya| Kawasaki, Mayu| Fujihara, Michiko| Watanabe, Masaki| Takamura, Yuta| Takioku, Maho| Nishioka, Hiromi| Takeuchi, Yasuo| Makishima, Makoto| Motoyama, Tomoharu| Ito, Sohei| Tokiwa, Hiroaki| Nakano, Shogo| Kakuta, Hiroki|
Note This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Medicinal Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jmedchem.9b00995.|
Published Date 2019-09-04
Publication Title Journal of Medicinal Chemistry
Volume volume62
Issue issue19
Publisher American Chemical Society
Start Page 8809
End Page 8818
ISSN 00222623
NCID AA00702411
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 American Chemical Society
File Version author
PubMed ID 31483660
DOI 10.1021/acs.jmedchem.9b00995
Web of Science KeyUT 000490355000010
Related Url isVersionOf https://doi.org/10.1021/acs.jmedchem.9b00995
FullText URL IntJMolSci_20_8_1973.pdf
Author Nakano, Keisuke| Takabatake, Kiyofumi| Kawai, Hotaka| Yoshida, Saori| Maeda, Hatsuhiko| Kawakami, Toshiyuki| Nagatsuka, Hitoshi|
Keywords cell differentiation epithelial-mesenchymal interaction immunohistochemistry malignant transformation notch signaling odontogenic tumor pleomorphic adenoma
Published Date 2019-04-23
Publication Title International Journal of Molecular Sciences
Volume volume20
Issue issue8
Publisher MDPI
Start Page 1973
ISSN 14220067
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 by the authors.
File Version publisher
PubMed ID 31018488
DOI 10.3390/ijms20081973
Web of Science KeyUT 000467648700171
Related Url isVersionOf https://doi.org/10.3390/ijms20081973
JaLCDOI 10.18926/AMO/57374
FullText URL 73_5_433.pdf
Author Tamada, Shoko| Mitsui, Takashi| Ohira, Akiko| Tani, Kazumasa| Maki, Jota| Eguchi, Takeshi| Eto, Eriko| Hayata, Kei| Masuyama, Hisashi|
Abstract An association between preeclampsia and (pro)renin was recently reported. Intracellular signaling of the (pro) renin receptor [(P)RR] increases the expressions of TGF-β and PAI-1. In this study we sought to clarify the involvement of (pro)renin in the pathogenesis of preeclampsia via the intracellular signaling of (P)RR on preeclampsia placentas. Activated (pro)renin plasma concentrations were compared between pregnant women with (n=15) and without (n=28) preeclampsia. The placentas were immunohistochemically evaluated with anti-HIF-1α and anti-(P)RR antibodies. HTR-8/SVneo cells were cultured under hypoxic conditions and treated with human recombinant (pro)renin. The mRNA expressions of HIF-1α, (P)RR, PAI-1, TGF-β, and ET-1 were also examined by real-time RCR. The activated (pro)renin plasma concentration was significantly higher in the third vs. the second trimester in the preeclampsia patients. HIF-1α and (P)RR expressions were significantly increased in the preeclampsia placentas. The mRNA expressions of PAI-1, TGF-β, and ET-1 were significantly increased in the experiments using recombinant (pro)renin vs. hypoxic conditions. (P)RR expression in preeclampsia placentas is increased by persistent hypoxia through the second and third trimesters, and PAI-1, TGF-β, and ET-1 production is increased via (P)RR. Our results suggest that ET-1 production via the intracellular signaling of (P)RR is important in the pathogenesis of preeclampsia.
Keywords preeclampsia (pro)renin (pro)renin receptor endothelin-1 HTR-8/SVneo
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 433
End Page 440
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649370
Web of Science KeyUT 000491886600009
JaLCDOI 10.18926/AMO/57370
FullText URL 73_5_403.pdf
Author Ando, Akemi| Mitsuhashi, Toshiharu| Honda, Mitsugi| Hanayama, Yoshihisa| Hasegawa, Kou| Obika, Mikako| Kataoka, Hitomi| Otsuka, Fumio|
Abstract Osteoporosis increases the risk of bone fractures. It is diagnosed based on an individual’s bone mineral density (BMD) or a fracture without trauma. BMD is usually measured by the dual energy X-ray absorptiometry (DXA) method. Here we investigated factors for the earliest possible prediction of decreased BMD by examining the relationships between patients’ BMD values and changes in the patients’ physical and laboratory values. We retrospectively reviewed the medical records of 149 patients who visited our department in 2014-2015 for a variety of reasons and underwent an area BMD examination by DXA. We analyzed the relationships between decreasing BMD and the patients’ gender, age, body mass index (BMI), medical background, hemoglobin, electrolytes, and thyroid function. Thirty-nine of the patients were diagnosed with osteoporosis based on their T-scores. An adjusted analysis showed that female gender, aging, and increased serum calcium level were significantly related to decreasing femoral BMD, whereas high BMI was associated with an increase in femoral BMD. Collectively the results indicate that for the early detection of low BMD, it is important for general-practice physicians to consider conducting a BMD checkup when treating female and elderly patients with a low BMI and/or elevated serum calcium level.
Keywords bone mineral density (BMD) body mass index (BMI) female gender hypercalcemia osteoporosis
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 403
End Page 411
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649366
Web of Science KeyUT 000491886600005
JaLCDOI 10.18926/AMO/56937
FullText URL 73_4_349.pdf
Author Isozaki, Hiroshi| Yamamoto, Yasuhisa| Murakami, Shigeki| Matsumoto, Sasau| Takama, Takehiro|
Abstract To clarify the surgical outcomes of breast cancer patients with a preoperative diagnosis of ductal carcinoma in situ (DCIS) by core needle biopsy (CNB) (abbreviated as CNBDCIS), we retrospectively analyzed the cases of 131 patients with CNBDCIS who underwent surgery at Oomoto Hospital (32 total mastectomies, 99 conservative mastectomies). Our analysis of underestimation and predictors of invasive breast cancer of CNBDCIS revealed that the underestimation rate of CNBDCIS was 40.5% (53/131). A logistic regression analysis revealed that palpable tumors (yes to no, odds ratio [OR] 3.25), mammography (MMG) category group (category 4 or 5 to categories 1 , 2, or 3, OR 4.69) and MMG microcalcifications (no to yes, OR 0.24) were significant predictive factors for CNBDCIS invasion. In our analysis of the predictors of positive margins during CNBDCIS surgery, 36 (27.5%) of the 131 patients had positive margins after postoperative pathological examination. A logistic regression analysis revealed that the operative procedure (conservative surgery to total mastectomy, OR 21.4) and MMG microcalcifications (yes to no, OR 3.35) were significant factors related to positive margins during CNBDCIS surgery. Thus, MMG microcalcifications are a negative predictor of upgrading of CNBDCIS and a positive predictor of positive surgical margins for CNBDCIS.
Keywords ductal carcinoma in situ core needle biopsy underestimation positive margins microcalcifications on mammography
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-08
Volume volume73
Issue issue4
Publisher Okayama University Medical School
Start Page 349
End Page 356
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31439958
JaLCDOI 10.18926/AMO/56934
FullText URL 73_4_325.pdf
Author Ueno, Tsuyoshi| Maki, Yuho| Sugimoto, Ryujiro| Suehisa, Hiroshi| Yamashita, Motohiro| Harada, Daijiro| Kozuki, Toshiyuki| Nogami, Naoyuki|
Abstract Therapeutic approaches to bronchopleural fistula (BPF) closure after lung resection are surgical or endoscopic interventions. We evaluated therapeutic outcomes to determine the optimal approach. We reviewed 15 patients who had developed BPF after lung resection for thoracic malignant diseases at our institution in the 10 years since 2008. The patients were 11 men and 4 women (mean age 68 years). We performed one pneumonectomy, 6 lobectomies, 7 segmentectomies, and one partial resection for malignant diseases. The median interval from lung resection to the BPF diagnosis was 46 days. The BPF-associated mortality rate was 26.7% (4/15). The rate of successful BPF closure was 66.6% (10/15). The endoscopic and surgical intervention success rates were 14.2% (1/7) and 69.2% (9/13), respectively (p<0.01). Of 5 patients who had failed BPF treatments, 4 died, and one transferred out without BPF closure. The therapeutic outcomes were related to preoperative comorbidities, performance status at the BPF diagnosis, time intervals from lung resection to BPF diagnosis, and presence of active pneumonia. The difference between endoscopic and surgical outcomes was nonsignificant, although the surgical intervention success rate was somewhat higher. The selection of endoscopic or surgical intervention for BPF does not significantly affect therapeutic outcomes.
Keywords bronchopleural fistula endoscopic intervention surgical intervention
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-08
Volume volume73
Issue issue4
Publisher Okayama University Medical School
Start Page 325
End Page 331
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31439955
JaLCDOI 10.18926/AMO/56930
FullText URL 73_4_285.pdf
Author Otani, Yoshihiro| Ichikawa, Tomotsugu| Kurozumi, Kazuhiko| Date, Isao|
Abstract Gliomas are characterized as highly diffuse infiltrating tumors, and currently available treatments such as surgery, radiation and chemotherapy are unfeasible or show limited efficacy against these tumors. Recent genetic and epigenetic analyses of glioma have revealed increasing evidence of the role of driver genetic alterations in glioma development and led to the identification of prognostic factors. Despite these findings, the survival rates of glioma patients remain low, and alternative treatments and novel targets are needed. Recent studies identified neural stem cells as the possible origin of gliomas, and some evidence has revealed shared functions and mechanisms between glioma cells and neurons, also supporting their similarity. The cytoskeleton plays important roles in the migration of normal cells as well as cancer cells. Recent reports have described a role for microtubules, a component of the cytoskeleton, in glioma invasion. Notably, several factors that regulate microtubule functions, such as microtubule-associated proteins, plus-end tracking proteins, or motor proteins, are upregulated in glioma tissues compared with normal tissue, and upregulation of these factors is associated with high invasiveness of glioma cells. In this review, we describe the mechanism of microtubules in glioma invasion and discuss the possibility of microtubule-targeted therapy to inhibit glioma invasion.
Keywords glioma cytoskeletons invasion microtubules
Amo Type Review
Publication Title Acta Medica Okayama
Published Date 2019-08
Volume volume73
Issue issue4
Publisher Okayama University Medical School
Start Page 285
End Page 297
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31439951
JaLCDOI 10.18926/AMO/56868
FullText URL 73_3_247.pdf
Author Yoshio, Kotaro| Wakita, Akihisa| Mitsuhashi, Toshiharu| Kitayama, Takahiro| Hisazumi, Kento| Inoue, Daisaku| Tajiri, Nobuhisa| Shiode, Tsuyoki| Akaki, Shiro| Kanazawa, Susumu|
Abstract We investigated the feasibility of simultaneous integrated boost (SIB) volumetric modulated arc therapy (VMAT) using elective nodal irradiation (ENI) for middle or lower esophageal cancer and compared it with three-dimensional conformal radiotherapy (3D-CRT). The study included 15 patients. The prescribed doses included a standard dose (50.4 Gy) and a high dose (60 Gy) for the planning target volume (PTV) of the involved lesions. The objective of the whole lung volume receiving ≥ 20 Gy (V20Gy) was < 30%, and the mean lung dose (MLD) was < 20 Gy. The volumes of the lung receiving 5 Gy (V5Gy) and the heart receiving 30-50 Gy (V30-50Gy) were kept as low as reasonably achievable. As a result, SIB-VMAT showed superior dose conformity for the PTV (p<0.001). Although the lung V5Gy was significantly increased (p<0.001), the V20Gy and MLD showed no significant increase. The heart V30-50Gy showed a > 20% reduction in the mean against 3D-CRTs. Our results demonstrate the feasibility of SIB-VMAT for the treatment of middle or lower esophageal cancer with ENI. Although attention should be paid to the low-dose area of the lungs, SIB-VMAT would be a promising treatment option with improved outcomes for esophageal cancer.
Keywords esophageal cancer middle and lower thoracic volumetric modulated arc therapy, 3D-CRT elective nodal irradiation
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-06
Volume volume73
Issue issue3
Publisher Okayama University Medical School
Start Page 247
End Page 257
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31235973
JaLCDOI 10.18926/AMO/56649
FullText URL 73_2_135.pdf
Author Maeba, Takahiro| Yonezawa, Tomoko| Ono, Mitsuaki| Tomono, Yasuko| Heljasvaara, Ritva| Pihlajaniemi, Taina| Inagawa, Kiichi| Oohashi, Toshitaka|
Abstract The basement membrane (BM) is composed of various extracellular molecules and regulates tissue regeneration and maintenance. Here, we demonstrate that collagen XVIII was spatiotemporally expressed in the BM during skin wound healing in a mouse excisional wound-splinting model. Re-epithelialization was detected at days 3 and 6 post-wounding. The ultrastructure of epidermal BM was discontinuous at day 3, whereas on day 6 a continuous BM was observed in the region proximal to the wound edge. Immunohistochemistry demonstrated that collagen XVIII was deposited in the BM zone beneath newly forming epidermis in day 3 and 6 wounds. Laminin-332, known to be the earliest BM component appearing in wounds, was colocalized with collagen XVIII in the epidermal BM zone at days 3 and 6. The deposition of α1(IV) collagen and nidogen-1 in the epidermal BM zone occurred later than that of collagen XVIII. We also observed the short isoform of collagen XVIII in the epidermal BM zone at day 3 post-wounding. Collectively, our results suggested that collagen XVIII plays a role in the formation of the dermal-epidermal junction during re-epithelialization, and that it is the short isoform that is involved in the early phase of re-epithelialization.
Keywords collagen XVIII basement membrane wound healing re-epithelialization skin
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-04
Volume volume73
Issue issue2
Publisher Okayama University Medical School
Start Page 135
End Page 146
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31015748
JaLCDOI 10.18926/56521
Title Alternative Intercultural Education for Japanese Students Using Revised Muslim Culture Assimilators
FullText URL scs_018_053_066.pdf
Author Nakano, Sachiko| Tanaka, Tomoko|
Publication Title Studies in Cultural Symbiotics
Published Date 2019-03-15
Volume volume18
Start Page 53
End Page 66
ISSN 1880-9162
language Japanese
Copyright Holders Copyright © 2019 岡山大学大学院社会文化科学研究科
File Version publisher
NAID 120006583681
JaLCDOI 10.18926/AMO/56464
FullText URL 73_1_85.pdf
Author Abe, Yoshiyuki| Fujibayashi, Kazutoshi| Nishizaki, Yuji| Yanagisawa, Naotake| Nojiri, Shuko| Nakano, Soichiro| Tada, Kurisu| Yamaji, Ken| Tamura, Naoto|
Abstract Pneumocystis pneumonia (PCP) due to Pneumocystis jirovecii infection is the leading cause of fatal opportunistic infections in immunocompromised patients. We will determine whether a daily sulfamethoxazole-trimethoprim (SMX/TMP) dose of 200/40 mg was non-inferior to 400/80 mg for PCP prevention in patients with systemic rheumatic disease under immunosuppressive therapy. This is a randomized, open-label, multicenter controlled trial. The primary outcome is the rate of PCP prevention at 52 weeks. The secondary outcome is the discontinuation rate of SMX/TMP. The trial will evaluate the optimal dose of SMX/TMP for PCP prevention in patients with systemic rheumatic disease under immunosuppressive therapy.
Keywords pneumocystis pneumonia prophylaxis systemic rheumatic disease sulfamethoxazole-trimethoprim conventional-dose versus half-dose
Amo Type Clinical Study Protocol
Publication Title Acta Medica Okayama
Published Date 2019-02
Volume volume73
Issue issue1
Publisher Okayama University Medical School
Start Page 85
End Page 89
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30820060
FullText URL PhysRevB_97_094525.pdf
Author Terashima, K.| Paris, E.| Simonelli, L.| Salas-Colera, E.| Puri, A.| Wakita, T.| Yamada, Y.| Nakano, S.| Idei, H.| Kudo, K.| Nohara, M.| Muraoka, Y.| Mizokawa, T.| Yokoya, T.| Saini, N. L.|
Note This is an article published by American Physical Society|
Published Date 2018-09-28
Publication Title Physical Review B
Volume volume98
Issue issue9
Publisher American Physical Society
Start Page 094525
ISSN 24699950
NCID AA11187113
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version publisher
DOI 10.1103/PhysRevB.98.094525
Web of Science KeyUT 000446178800008
Related Url isVersionOf https://doi.org/10.1103/PhysRevB.98.094525